ENST00000248633.9:c.2346A>G
MANE Select
|
ENSP00000248633.4:p.Arg782=
|
|
ENST00000248633.8:c.2346A>G
|
ENSP00000248633.4:p.Arg782=
|
|
ENST00000428214.5:c.2175A>G
|
ENSP00000394413.1:p.Arg725=
|
|
ENST00000438045.5:c.1380A>G
|
ENSP00000410438.1:p.Arg460=
|
|
ENST00000484913.5:n.2385A>G
|
|
|
ENST00000496092.1:n.144A>G
|
|
|
ENST00000496420.5:n.2022A>G
|
|
|
NM_000466.2:c.2346A>G
|
NP_000457.1:p.Arg782=
|
|
NM_001282677.1:c.2175A>G
|
NP_001269606.1:p.Arg725=
|
|
NM_001282678.1:c.1722A>G
|
NP_001269607.1:p.Arg574=
|
|
XM_005250433.3:c.597A>G
|
XP_005250490.1:p.Arg199=
|
|
XR_242246.3:n.2442A>G
|
|
|
XM_017012319.2:c.597A>G
|
XP_016867808.1:p.Arg199=
|
|
XR_001744808.2:n.1373A>G
|
|
|
XR_242246.5:n.2393A>G
|
|
|
NM_000466.3:c.2346A>G
MANE Select
|
NP_000457.1:p.Arg782=
|
|
NM_001282677.2:c.2175A>G
|
NP_001269606.1:p.Arg725=
|
|
NM_001282678.2:c.1722A>G
|
NP_001269607.1:p.Arg574=
|
|